Senior Clinical Process Manager
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Do you want to be part of an exciting journey?
Do you have clinical process development experience, and are you looking for a job where you can put your strong knowledge into play to ensure operational excellence of clinical trials across different functional areas in an innovative global company? Then this job might be something for you.
LEO Pharma has set the ambitious goal to become the world’s preferred dermatology care partner and to improve the quality of life for millions of patients around the world. To succeed, we invest massively in Research & Development. As a result, our pipeline and clinical activities are growing rapidly, constantly demanding a strong and continued focus on driving efficiencies and optimisations in our organisation, and that is why we need you!
If you are an experienced project manager with a strong knowledge of drug development processes, tools and systems, and you are looking for a job where you can unfold all your skills in a role with great impact and influence in a growing innovative company, you are the perfect match!
About the job – delivering high quality clinical processes
As Senior Process Manager in Clinical Process Management your overall objective is to support the continuous improvement and development of efficient, high quality and compliant processes supporting the operational excellence in Global Clinical Operations and Medical Sciences. Besides, support an agile working environment with digitalisation of clinical trials on the agenda.
In this role you will lead process optimisation from definition, planning, execution, management of deliverables to training and implementation in close collaboration with subject matter experts across the organisation.
Your primary tasks will be to:
- Drive and identify opportunities for continuous process improvement involving both systems, tools, and processes in in close collaboration with key stakeholders across the organization
- Lead and participate in process improvements projects
- Drive and facilitate workshops to support continuous process improvement
- Proactively facilitate and communicate lessons learned and best practices
- Support operational excellence through continuous stakeholder management and communication
- Communicate and report to Steering Committee or Leadership Teams
We are offering a job with considerable individual responsibility and challenges, and a high level of visibility, as you will collaborate with a great number of stakeholders across the organization.
About you – an experienced process manager
You are an experienced project manager with a master in natural or life science like Pharmacy or equivalent relevant education. Ideally you have at least 5 years’ hands-on working experience within the clinical drug development discipline. Further, you are able to demonstrate solid experience in driving and implementing process optimisations within R&D in the pharmaceutical industry. As part of your PM toolbox, you know how to apply LEAN methodologies and effective change management.
To succeed in the job, you use your personal impact and pro-active can-do attitude to achieve long-lasting results and secure end-to-end thinking. You recognise the importance of building relationships across the organization and benefit from your excellent communication skills that enable you to bring your messages across in an easily understandable way, written and spoken. You are an excellent collaborator with a supportive mindset, who have the ability to motivate and inspire others.
Becoming part of an organization constantly developing, you must enjoy and embrace an environment of change and take a pragmatic approach to problem-solving.
About Clinical Process Management – your new department
Clinical Process Management is one of four departments in Clinical Operations Support within Global Clinical Operations. We strive to support our internal stakeholders with processes, training, and compliance to deliver high-quality clinical trials. The department consist of ten dedicated process and compliance specialists with high professional standards. The working atmosphere is busy, collegial, and informal, and as for the rest of LEO Pharma, innovation is part of everything we do.
We look forward to receiving your application before the 20th of January 2022. However, we will be screening and interviewing an on-going basis.
For more information, please contact Trine Danø Klingberg, Head of Clinical Process Management on +45 3126 2553.
LEO Pharma
LEO Pharma is on an exciting journey of transformation to become the world leader in dermatology. We keep the patients at the heart of everything we do, and we drive dermatology with our knowledge, collaboration and curiosity. We are at the forefront of science in developing new medicines for dermatology, and we are committed to helping people with skin diseases live more fulfilling lives.
Our people are united worldwide with strong core values and a common vision. Our shared vision and mission adapt to an ever-changing environment, while remaining true to our business strategy. Our values reflect the way we strive to increase the quality of life for patients.
Founded in 1908 and owned by the LEO Foundation, LEO Pharma has devoted decades of research and development to advance the science of dermatology, setting new standards of care for people with skin conditions.
LEO Pharma is headquartered in Denmark with a global team of 6,000 people, serving 92 million patients in 130 countries
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 14.12.2021, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Projektleder
- Ballerup
- Søndag den 09. januar 2022
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